Canonical Allele Identifier: CA2293845719
Gene: DSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31498278C= , CM000680.2:g.31498278C= GRCh38
NC_000018.9:g.29078241C= , CM000680.1:g.29078241C= GRCh37
NC_000018.8:g.27332239C= NCBI36
NG_007072.3:g.5037C= , LRG_397:g.5037C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682241.2:c.27C= ENSP00000507600.2:p.Tyr9=
ENST00000683654.1:c.27C= ENSP00000506971.1:p.Tyr9=
ENST00000261590.13:c.27C= MANE Select ENSP00000261590.8:p.Tyr9=
ENST00000261590.12:c.27C= ENSP00000261590.8:p.Tyr9=
ENST00000585206.1:c.27C= ENSP00000462503.1:p.Tyr9=
NM_001943.3:c.27C= , LRG_397t1:c.27C= NP_001934.2:p.Tyr9=
NM_001943.4:c.27C= NP_001934.2:p.Tyr9=
NM_001943.5:c.27C= MANE Select NP_001934.2:p.Tyr9=